Evidence map›Paper›PMID 33484826›Full record

ArticleMethods (San Diego, Calif.)2021

Prediction and interpretation of cancer survival using graph convolution neural networks.

Ricardo Ramirez, Yu-Chiao Chiu, SongYao Zhang, Joshua Ramirez, Yidong Chen, Yufei Huang, Yu-Fang Jin

Open access · greenAbstract read
In one paragraph

Article in Methods (San Diego, Calif.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
4.1field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Ricardo RamirezDepartment of Electrical and Computer Engineering, The University of Texas at San Antonio, San Antonio, TX 78249, USA.
Yu-Chiao ChiuGreehey Children's Cancer Research Institute, The University of Texas Health San Antonio, San Antonio, Texas 78229, USA.
SongYao ZhangKey Laboratory of Information Fusion Technology of Ministry of Education, Department of Intelligent Science And Technology, School of Automation, Northwestern Polytechnical University, Xí'an, China.
Joshua RamirezDepartment of Electrical and Computer Engineering, The University of Texas at San Antonio, San Antonio, TX 78249, USA.
Yidong ChenGreehey Children's Cancer Research Institute, The University of Texas Health San Antonio, San Antonio, Texas 78229, USA; Department of Population Health Sciences, The University of Texas Health San Antonio, San Antonio, TX 78229, USA.
Yufei HuangDepartment of Electrical and Computer Engineering, The University of Texas at San Antonio, San Antonio, TX 78249, USA; Department of Population Health Sciences, The University of Texas Health San Antonio, San Antonio, TX 78229, USA.
Yu-Fang JinDepartment of Electrical and Computer Engineering, The University of Texas at San Antonio, San Antonio, TX 78249, USA. Electronic address: yufang.jin@utsa.edu.
The University of Texas at San Antonio · USThe University of Texas Health Science Center at San Antonio · USNorthwestern Polytechnical University · CN

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUM1TR004538 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ROBERT A CLARK, Kenneth M Hargreaves · 2023 to 2026
$22.3M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR002645 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2018 to 2022
$20.4M
Collaborative Research:Graphical models for characterizing global RNA methylationR01GM113245 · NIGMS · UNIVERSITY OF TEXAS SAN ANTONIO · PI HUANG, YUFEI · 2014 to 2016
$1.1M
Deep learning of drug sensitivity and genetic dependency of pediatric cancer cellsK99CA248944 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CHIU, YU-CHIAO · 2020 to 2021
$212k
NCATS NIH HHS UL1 TR002645NCATS NIH HHS UM1 TR004538NCI NIH HHS K99 CA248944NCI NIH HHS P30 CA054174NIGMS NIH HHS R01 GM113245
6 · The paper itself

Abstract

The survival rate of cancer has increased significantly during the past two decades for breast, prostate, testicular, and colon cancer, while the brain and pancreatic cancers have a much lower median survival rate that has not improved much over the last forty years. This has imposed the challenge of finding gene markers for early cancer detection and treatment strategies. Different methods including regression-based Cox-PH, artificial neural networks, and recently deep learning algorithms have been proposed to predict the survival rate for cancers. We established in this work a novel graph convolution neural network (GCNN) approach called Surv_GCNN to predict the survival rate for 13 different cancer types using the TCGA dataset. For each cancer type, 6 Surv_GCNN models with graphs generated by correlation analysis, GeneMania database, and correlation + GeneMania were trained with and without clinical data to predict the risk score (RS). The performance of the 6 Surv_GCNN models was compared with two other existing models, Cox-PH and Cox-nnet. The results showed that Cox-PH has the worst performance among 8 tested models across the 13 cancer types while Surv_GCNN models with clinical data reported the best overall performance, outperforming other competing models in 7 out of 13 cancer types including BLCA, BRCA, COAD, LUSC, SARC, STAD, and UCEC. A novel network-based interpretation of Surv_GCNN was also proposed to identify potential gene markers for breast cancer. The signatures learned by the nodes in the hidden layer of Surv_GCNN were identified and were linked to potential gene markers by network modularization. The identified gene markers for breast cancer have been compared to a total of 213 gene markers from three widely cited lists for breast cancer survival analysis. About 57% of gene markers obtained by Surv_GCNN with correlation + GeneMania graph either overlap or directly interact with the 213 genes, confirming the effectiveness of the identified markers by Surv_GCNN.

Indexed as

Neural Networks, ComputerAlgorithmsBreast NeoplasmsHumansMaleSurvival RateGraph convolutional neural networkSurvival analysisThe cancer genome atlas (TCGA)

Identifiers

PMID33484826
PMCPMC8808665
OpenAlexW3121756359

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.